A Phase 3b Study to Evaluate the Duration of Effect of Bimatoprost SR in Participants With Open-Angle Glaucoma or Ocular Hypertension

  • End date
    Jun 30, 2025
  • participants needed
  • sponsor
Updated on 22 October 2022
brimonidine tartrate ophthalmic solution
intraocular pressure
pigmentary glaucoma
pseudoexfoliation glaucoma


This study evaluates the duration of intraocular pressure (IOP)-lowering effect and safety of as needed administrations of Bimatoprost sustained release (SR) in participants with open-angle glaucoma (OAG) or ocular hypertension (OHT) who are not adequately managed with topical IOP-lowering medication for reasons other than medication efficacy.

Condition Open-Angle Glaucoma, Ocular Hypertension
Treatment Bimatoprost (SR)
Clinical Study IdentifierNCT03850782
Last Modified on22 October 2022


Yes No Not Sure

Inclusion Criteria

Diagnosis of either Diagnosis of either open angle glaucoma (OAG) (i.e., primary OAG, pseudoexfoliation glaucoma, pigmentary glaucoma) or ocular hypertension requiring intraocular pressure-lowering treatment

Exclusion Criteria

Concurrent or anticipated enrollment in another investigational drug or device study or participation in such a study within 2 months prior to enrolling in this study
Previous administration with Bimatoprost SR in the study eye
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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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